| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:807845-808187 | Common:2; Rare:109 | ||||
| chr19:913165-913278 | Rare:36 | ||||
| chr19:1021204-1021517 | Common:13; Rare:127 | ||||
| chr19:1066891-1067215 | Common:4; Rare:82 | ||||
| chr19:1103749-1104114 | Common:7; Rare:153 | ||||
| chr19:1132137-1132478 | Common:2; Rare:142 | ||||
| chr19:1207117-1207314 | Common:3; Rare:70; Clinvar:3; Clinvar (benign):20; Clinvar (pathogenic):1 | ||||
| chr19:1251433-1251672 | Rare:101 | ||||
| chr19:1251743-1251815 | Common:1; Rare:28 | ||||
| chr19:1269040-1269357 | Common:2; Rare:119 | ||||
| chr19:1275636-1276091 | Common:2; Rare:221 | ||||
| chr19:1942086-1942484 | Rare:124 | ||||
| chr19:1942812-1942908 | Rare:23 | ||||
| chr19:2085268-2085523 | Common:4; Rare:66 | ||||
| chr19:2096207-2096430 | Rare:75 |